The Fertilisers (Sampling and Analysis) Regulations 1991

PROCEDURE

Extraction

7.—7.1 Weigh to the nearest 0.001 g, 5 g of the prepared sample and place in a 500 ml graduated flask. Add about 300 ml water and boil for half an hour. Allow to cool, dilute to the mark with water, mix and filter.

Preparation of the sample solution

7.2 7.2.1 If the fertiliser has a declared magnesium oxide (MgO) content greater than 10%, transfer by pipette 25 ml of the filtrate (7.1) into a 100 ml graduated flask, make up to the mark with water and mix.

7.2.2 Transfer by pipette 10 ml of the filtrate (7.1) or the diluted filtrate (7.2.1) into a 200 ml graduated flask and make up to the mark with 0.5 N hydrochloric acid solution (4.2).

7.2.3 Dilute solution (7.2.2) with 0.5 N hydrochloric acid solution (4.2) to a concentration within the working range of the spectrophotometer.

• The final solution must contain 10% V/V of the strontium chloride solution (4.4).

Blank solution

7.3 Prepare a blank solution from which only the sample has been omitted.

Standard solutions for calibration

7.4 By diluting the standard solution (4.3) with 0.5 N hydrochloric acid solution (4.2), prepare at least 5 standard solutions of increasing concentration corresponding to the optimal measuring range of the spectrophotometer. The final solutions must contain 10% V/V of the strontium chloride solution (4.4).

Measurement

7.5 Set up the spectrophotometer (5.1), at a wavelength of 28.25 nm using an oxidising air-acetylene flame. Spray successively, in triplicate, the standard solutions (7.4), the sample solution (7.2) and the blank solution (7.3), washing the instrument through with distilled water between each spraying. Plot the calibration curve using the mean absorbances as the ordinates and the corresponding concentrations of magnesium in Ö as the abscissae. Determine the concentration of magnesium in the sample and blank by reference to the claibration curve.